JPH0567439B2 - - Google Patents
Info
- Publication number
- JPH0567439B2 JPH0567439B2 JP13145584A JP13145584A JPH0567439B2 JP H0567439 B2 JPH0567439 B2 JP H0567439B2 JP 13145584 A JP13145584 A JP 13145584A JP 13145584 A JP13145584 A JP 13145584A JP H0567439 B2 JPH0567439 B2 JP H0567439B2
- Authority
- JP
- Japan
- Prior art keywords
- ink
- porous powder
- impregnated
- powder particles
- melting
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000843 powder Substances 0.000 claims description 33
- 238000002844 melting Methods 0.000 claims description 14
- 239000002245 particle Substances 0.000 claims description 12
- 239000011230 binding agent Substances 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 239000012943 hotmelt Substances 0.000 claims description 7
- 239000000463 material Substances 0.000 claims description 7
- 239000002904 solvent Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000000976 ink Substances 0.000 description 39
- 229920005989 resin Polymers 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 6
- 238000005470 impregnation Methods 0.000 description 5
- 238000007639 printing Methods 0.000 description 5
- 239000000123 paper Substances 0.000 description 4
- 239000003086 colorant Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 238000005054 agglomeration Methods 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 229920000298 Cellophane Polymers 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004962 Polyamide-imide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 239000011086 glassine Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- -1 polypropylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/382—Contact thermal transfer or sublimation processes
- B41M5/38278—Contact thermal transfer or sublimation processes using ink-containing structures, e.g. porous or microporous layers, alveoles or cellules
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/913—Material designed to be responsive to temperature, light, moisture
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/914—Transfer or decalcomania
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31801—Of wax or waxy material
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
- Impression-Transfer Materials And Handling Thereof (AREA)
Description
[産業上の利用分野]
本発明は、サーマルプリンターやサーマルタイ
プライターなどの記録装置に使用され、熱溶融性
のインクが、サーマルヘツドによる加熱にて徐々
に記録紙などの受容体に転移することで、同一箇
所を多数回使用することができる、多数回使用型
熱転写記録媒体の製法に関する。
[従来の技術]
従来この種の多数回使用型熱転写記録媒体とし
ては、熱溶融性のインクに対し非相溶性の樹脂を
用い、この樹脂にて形成されるスポンジ層内に前
記インクが含有せしめられている構成のものと、
凝集性の強い微粉体を前記インクに混合しこの微
粉体の凝集によつて形成されたバリヤー層を設け
たものとが知られている。
[発明が解決しようとする問題点]
しかし、前者のものでは、スポンジ層を形成す
る樹脂中に包み込まれるようにインクが保持され
ているので、初期の印像形成濃度が薄く、濃度の
高い鮮明な印像をうることができなかつた。
また、後者のものでは、凝集している微粉末間
の空隙率が小さいために保有するインク量が少な
く、そのため印字濃度が低く、かつ印字回数も少
なかつた。
本発明は、このような実情に鑑み、前記欠点を
解消することを目的とする。
[問題点を解消するための手段]
そして、この目的を達成するために、本発明
は、空隙率50〜97%の多孔質粉体粒子に熱溶融性
インクを含浸せしめ、ついで該インク含浸多孔質
粉体粒子を、前記熱溶融性インクに対し実質的に
非相溶性のバインダー剤の溶剤溶液に分散せしめ
たものを基材上に塗布、乾燥して、基材上に前記
インク含浸多孔質粉体粒子が前記バインダー剤に
て相互に結合されてなるインク含有層を形成する
構成としたものである。
[作用]
このように構成することにより、熱溶融性イン
クは、サーマルヘツドの加熱により溶融して多孔
質粉体から徐々ににじみ出し、記録紙などの受容
体に転移して印像を形成することとなる。
[効果]
その結果、前記従来のスポンジ層のものに比
べ、樹脂にインクが抱き込まれるようなことがな
く、低い熱エネルギーで熱溶融性インクが受容体
に転移する点で有利であり、また前記従来の凝集
微粉体によるものに比べ、インク保持率が高く、
濃度の高い印字が持続してえられるに至つた。
これらにより、従来のものに比べて、初期印像
濃度が高くかつその高濃度での印像が持続する良
好な多数回使用が可能となつた。
[実施態様]
つぎに本発明を具体的に説明する。
前記多孔質粉体としては、平均粒子径が1〜
20μmで、空隙率が50〜97%、とくに60〜93%の
ものが適当である。ここで空隙率とは粉体粒子の
全体積に対する空隙の体積の割合の平均値であ
る。前記平均粒子径が1μmより小さいと、ほとん
どの粉体の表面がバインダー剤により覆われ、イ
ンクがにじみださなくなる。また平均粒子径が
20μmより大きいと、印像の一部に欠けが生じ印
字品位が低下する。空隙率が50%より小さいと、
使用回数が著しく低下するのみならず、使用につ
れて印字濃度が急激に低下する。また、空隙率が
97%より大きいと、粉体の剛性が小さくなり、バ
インダー剤との混合時に壊れてしまう惧れがあ
る。
この多孔質粉体の例としては、珪藻土、ゼオラ
イト、ベントナイトなどの無機多孔質粉体、ウレ
タンポアパウダーなどの有機多孔質粉体があげら
れる。
バインダー剤としては、前記熱溶融性インクに
対し非相溶性または難相溶性であつて、記録媒体
の基材や多孔質粉体に対し接着性を有し、サーマ
ルヘツドの加熱により溶融しないものがよく、た
とえばポリエスル樹脂、エポキシ樹脂、スチレン
樹脂、ポリカーボレネート樹脂、セルロースアセ
テートブチレート、エチルセルロース、ポリアミ
ドイミド樹脂などの軟化点が70℃以上の熱溶融性
樹脂または熱硬化性樹脂があげられる。これら樹
脂は単独で用いてもよく、2種以上を併用しても
よい。また、適当な添加物を目的に応じ1種また
は2種以上適量添加してもよい。
これらバインダー剤は、前記多孔質粉体10重量
部に対し、1〜15重量部程度配合するのが適当で
ある。
前記熱溶融性のインクとしては、従来より熱転
写用記録媒体の固形インクとして通常用いられて
いるものと同様な成分のものが使用できるが、と
くに溶融温度より30℃高い温度における粘度が10
〜500cP(B型粘度計による測定値)であつて、
溶融温度が50〜120℃のものが適当であり、前記
バインダー剤の軟化点より低く調整してあるもの
がよい。熱溶融性インクの着色剤としてはカーボ
ンブラツクなどの黒色顔料のみならず、青、赤、
黄などの着色剤を使用してカラーの印像を形成し
うるようにしてもよい。これらカラーの着色剤と
しては従来のワンタイム熱転写記録媒体に用いら
れているものがいずれも使用できる。
この熱溶融性インクは、前記多孔質粉体5重量
部に対し、3〜20重量部程度配合するのが適当で
ある。
熱溶融性のインクを加熱溶融したところの液状
のインクを多孔質粉体に含浸させるには、つぎの
方法がある。
1つの方法は溶融したインクと多孔質粉体とを
デスパーなどの混合器に入れて混合することによ
つてインクを粉体内に含浸させる方法であり、他
の方法は溶融したインクと多孔質粉体とを混ぜ合
せたのち真空含浸装置で真空含浸させる方法であ
る。
これらの方法で熱溶融性インクが含浸された多
孔質粉体を、該インクが熱溶融された状態で前記
バインダー剤の溶液(用いる溶剤は、前記熱溶融
性インクと多孔質粉体とをほとんど溶解しないも
のがよい)と混合して、基材に塗布し、乾燥して
インク含含層を形成する。該インク層の乾燥後の
厚さは1〜20μmが適当である。
前記基材としては、ポリエステル、ポリカーボ
ネート、ナイロン、ポリプロピレンなどのプラス
チツクフイルム、防湿セロハン、コンデンサー
紙、グラシン紙などの高密度紙、あるいはこれら
の片面または両面に金属を蒸着またはラミネート
した薄厚のシートなどが用いられる。
[実施例]
つぎに実施例をあげて本発明を説明する。
実施例1〜4および比較例1〜2
第1表に示される多孔質粉体に第2表に示され
る熱溶融性インクを含浸させた。インクの含浸は
熱溶融したインクと多孔質粉体とを混合し、真空
含浸装置で真空含浸させることによつて行なつ
た。このようにしてインクを含浸した多孔質粉体
を該インクが熱溶融された状態で第1表に示され
るバインダー剤溶液と混合し、えられた混合液を
第1表に示される基材上に塗布し、乾燥して溶剤
を除去することによつて、第1表に示される厚さ
のインク含有層を形成した。
[Industrial Application Field] The present invention is used in recording devices such as thermal printers and thermal typewriters, in which heat-melting ink is gradually transferred to a receptor such as recording paper by heating with a thermal head. The present invention relates to a method for producing a multiple-use thermal transfer recording medium that can be used multiple times at the same location. [Prior Art] Conventionally, this type of multi-use thermal transfer recording medium uses a resin that is incompatible with heat-melting ink, and the ink is contained in a sponge layer formed of this resin. with the configuration that is
It is known that a highly cohesive fine powder is mixed with the ink and a barrier layer formed by the agglomeration of the fine powder is provided. [Problems to be Solved by the Invention] However, in the former method, the ink is held so as to be wrapped in the resin that forms the sponge layer, so the initial density of the formed image is low, and the ink is not formed with high density and sharpness. I couldn't get a good impression. Further, in the latter case, since the porosity between the aggregated fine powders was small, the amount of ink retained was small, resulting in low printing density and a small number of printings. In view of these circumstances, the present invention aims to eliminate the above-mentioned drawbacks. [Means for Solving the Problems] In order to achieve this object, the present invention impregnates porous powder particles with a porosity of 50 to 97% with a hot melt ink, and then inks the ink-impregnated porous particles. Fine powder particles are dispersed in a solvent solution of a binder agent that is substantially incompatible with the heat-melting ink, and then applied onto a base material and dried to form a porous layer impregnated with the ink on the base material. The ink-containing layer is formed by combining powder particles with each other using the binder agent. [Function] With this configuration, the heat-melting ink is melted by the heating of the thermal head, gradually oozes out from the porous powder, and is transferred to a receptor such as recording paper to form an image. It happens. [Effects] As a result, compared to the conventional sponge layer, the ink is not trapped in the resin, and the heat-melting ink is transferred to the receptor with low thermal energy, which is advantageous. Compared to the conventional method using agglomerated fine powder, the ink retention rate is higher,
Printing with high density can be achieved continuously. As a result, compared to conventional products, the initial print density is high and the print image at that high density lasts, making it possible to use the printhead many times. [Embodiments] Next, the present invention will be specifically explained. The porous powder has an average particle diameter of 1 to
A material with a diameter of 20 μm and a porosity of 50 to 97%, particularly 60 to 93% is suitable. Here, the porosity is the average value of the ratio of the volume of voids to the total volume of powder particles. When the average particle diameter is smaller than 1 μm, most of the surface of the powder is covered with the binder agent, and the ink does not bleed out. Also, the average particle size
If it is larger than 20 μm, part of the printed image will be chipped and the printing quality will deteriorate. If the porosity is less than 50%,
Not only does the number of uses decrease significantly, but the print density also decreases rapidly with use. In addition, the porosity
When it is greater than 97%, the rigidity of the powder decreases and there is a risk that it will break when mixed with the binder agent. Examples of this porous powder include inorganic porous powders such as diatomaceous earth, zeolite, and bentonite, and organic porous powders such as urethane pore powder. The binder agent is one that is incompatible or poorly compatible with the heat-melting ink, has adhesive properties to the base material of the recording medium and porous powder, and does not melt when heated by the thermal head. Common examples include heat-melting resins or thermosetting resins having a softening point of 70° C. or higher, such as polyester resins, epoxy resins, styrene resins, polycarbonate resins, cellulose acetate butyrate, ethyl cellulose, and polyamideimide resins. These resins may be used alone or in combination of two or more. In addition, one or more kinds of suitable additives may be added in appropriate amounts depending on the purpose. It is appropriate that these binder agents be blended in an amount of about 1 to 15 parts by weight per 10 parts by weight of the porous powder. As the heat-melting ink, those having the same composition as those conventionally used as solid inks for thermal transfer recording media can be used, but in particular those having a viscosity of 10°C at a temperature 30°C higher than the melting temperature can be used.
~500cP (measured value using a B-type viscometer),
It is suitable that the melting temperature is 50 to 120°C, and preferably adjusted to be lower than the softening point of the binder agent. Coloring agents for hot-melt ink include not only black pigments such as carbon black, but also blue, red,
A coloring agent such as yellow may be used to form a colored image. As these coloring agents, any of those used in conventional one-time thermal transfer recording media can be used. Appropriately, this heat-melting ink is blended in an amount of about 3 to 20 parts by weight based on 5 parts by weight of the porous powder. The following method can be used to impregnate porous powder with liquid ink obtained by heating and melting hot-melt ink. One method is to impregnate the ink into the powder by placing the molten ink and porous powder in a mixer such as a despar and mixing them, and the other method is to mix the molten ink and porous powder in a mixer such as a desper. This is a method of vacuum impregnation using a vacuum impregnation device after mixing with the body. The porous powder impregnated with the hot-melt ink by these methods is heated in a state in which the ink is hot-melted, and then the binder agent solution (the solvent used is almost the same as the hot-melt ink and the porous powder). (preferably one that does not dissolve) is applied to a substrate and dried to form an ink-containing layer. The thickness of the ink layer after drying is suitably 1 to 20 μm. Examples of the base material include plastic films such as polyester, polycarbonate, nylon, and polypropylene, high-density papers such as moisture-proof cellophane, condenser paper, and glassine paper, or thin sheets with metal vapor-deposited or laminated on one or both sides thereof. used. [Example] Next, the present invention will be described with reference to Examples. Examples 1 to 4 and Comparative Examples 1 to 2 The porous powders shown in Table 1 were impregnated with the hot melt inks shown in Table 2. Impregnation with ink was carried out by mixing hot molten ink and porous powder and vacuum impregnation using a vacuum impregnation device. The porous powder impregnated with the ink in this manner is mixed with the binder solution shown in Table 1 in a state in which the ink is thermally melted, and the resulting mixture is applied to the substrate shown in Table 1. An ink-containing layer having the thickness shown in Table 1 was formed by coating and drying to remove the solvent.
【表】【table】
【表】【table】
【表】
注1:オリエント化学(株)製のオイル染料
前記実施例1〜4でえられた多数回使用熱転写
記録媒体をキヤノン(株)製のサーマルプリンター
(WP−55)に使用し、記録媒体の同一箇所を用
い白色の記録紙に10回印字し、マクベス濃度計に
より各印像のOD値を測定した。結果を第3表に
示す。
また比較のために、特開昭54−68253号公報の
実施例1に示されるスポンジ層型の多数回使用熱
転写記録媒体(比較例1)および特開昭57−
160691号公報の例1に示される微粉体凝集型の多
数回使用熱転写記録媒体(比較例2)を用い、前
記と同様にして印像を形成して、マクベス濃度計
により各印像のOD値を測定した。結果を第3表
に示す。[Table] Note 1: Oil dye manufactured by Orient Chemical Co., Ltd. The multi-use thermal transfer recording media obtained in Examples 1 to 4 above were used in a thermal printer (WP-55) manufactured by Canon Inc. to perform recording. Printing was performed 10 times on white recording paper using the same location on the medium, and the OD value of each print was measured using a Macbeth densitometer. The results are shown in Table 3. For comparison, a sponge layer type multi-use thermal transfer recording medium (Comparative Example 1) shown in Example 1 of JP-A-54-68253 and JP-A-57-
Using the fine powder agglomeration type multi-use thermal transfer recording medium (Comparative Example 2) shown in Example 1 of Publication No. 160691, impressions were formed in the same manner as above, and the OD value of each impression was determined using a Macbeth densitometer. was measured. The results are shown in Table 3.
【表】【table】
【表】
なお、従来のワンタイム熱転写インクリボンを
使用して印像を形成したばあい、初回の印像の
OD値は1.1〜1.3であつた。[Table] When forming an image using a conventional one-time thermal transfer ink ribbon, the initial
The OD value was 1.1-1.3.
Claims (1)
インクを含浸せしめ、ついで該インク含浸多孔質
粉体粒子を、前記熱溶融性インクに対し実質的に
非相溶性のバインダー剤の溶剤溶液に分散せしめ
たものを基材上に塗布、乾燥して、基材上に前記
インク含浸多孔質粉体粒子が前記バインダー剤に
て相互に結合されてなるインク含有層を形成する
ことを特徴とする多数回使用型熱転写記録媒体の
製法。 2 溶融された前記熱溶融性インクを前記多孔質
粉体粒子に真空含浸せしめる特許請求の範囲第1
項記載の製法。[Scope of Claims] 1. Porous powder particles having a porosity of 50 to 97% are impregnated with a heat-melting ink, and then the ink-impregnated porous powder particles are substantially non-stick to the heat-melting ink. A compatible binder agent dispersed in a solvent solution is applied onto a base material and dried, and the ink-impregnated porous powder particles are bonded to each other by the binder agent on the base material. A method for producing a multi-use thermal transfer recording medium characterized by forming a layer. 2. Claim 1, wherein the porous powder particles are vacuum impregnated with the melted hot-melt ink.
Manufacturing method described in section.
Priority Applications (13)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59131455A JPS6110490A (en) | 1984-06-26 | 1984-06-26 | Repeatedly usable type thermal transfer recording medium |
US06/746,352 US4612243A (en) | 1984-06-26 | 1985-06-19 | Reusable heat-sensitive transfer element |
CA000484631A CA1237280A (en) | 1984-06-26 | 1985-06-20 | Re-using heat-sensitive transfer recording media |
DK280785A DK280785A (en) | 1984-06-26 | 1985-06-21 | RECYCLABLE REGISTRATION MEDIUM TRANSFERED ON HEAT SENSITIVITY |
DE19853522316 DE3522316A1 (en) | 1984-06-26 | 1985-06-21 | REUSABLE HEAT SENSITIVE TRANSFER RECORDING MEDIUM |
GB8515963A GB2161950B (en) | 1984-06-26 | 1985-06-24 | Re-using heat-sensitive transfer recording media |
AU43996/85A AU585868B2 (en) | 1984-06-26 | 1985-06-24 | Re-using heat-sensitive transfer recording media |
SE8503124A SE467818B (en) | 1984-06-26 | 1985-06-24 | ACCEPTABLE, EASY TRANSFER REGISTRATION MEDIUM |
CH2697/85A CH670422A5 (en) | 1984-06-26 | 1985-06-25 | |
IT2127585A IT1200648B (en) | 1984-06-26 | 1985-06-25 | REUSABLE THERMAL SENSITIVE TRANSFER REGISTRATION MEANS |
FR8509729A FR2566328B1 (en) | 1984-06-26 | 1985-06-26 | REUSABLE MEDIUM FOR THERMAL DEFERRAL RECORDING |
NL8501842A NL8501842A (en) | 1984-06-26 | 1985-06-26 | REPEATED USEFUL HEAT SENSITIVE TRANSFER DISPLAY MEDIUM. |
KR8504559A KR900005831B1 (en) | 1984-06-26 | 1985-06-26 | Re- using heat-sensitive transfer recording media |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59131455A JPS6110490A (en) | 1984-06-26 | 1984-06-26 | Repeatedly usable type thermal transfer recording medium |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6110490A JPS6110490A (en) | 1986-01-17 |
JPH0567439B2 true JPH0567439B2 (en) | 1993-09-24 |
Family
ID=15058355
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59131455A Granted JPS6110490A (en) | 1984-06-26 | 1984-06-26 | Repeatedly usable type thermal transfer recording medium |
Country Status (13)
Country | Link |
---|---|
US (1) | US4612243A (en) |
JP (1) | JPS6110490A (en) |
KR (1) | KR900005831B1 (en) |
AU (1) | AU585868B2 (en) |
CA (1) | CA1237280A (en) |
CH (1) | CH670422A5 (en) |
DE (1) | DE3522316A1 (en) |
DK (1) | DK280785A (en) |
FR (1) | FR2566328B1 (en) |
GB (1) | GB2161950B (en) |
IT (1) | IT1200648B (en) |
NL (1) | NL8501842A (en) |
SE (1) | SE467818B (en) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4784905A (en) * | 1985-03-01 | 1988-11-15 | Ricoh Company, Ltd. | Thermosensitive image transfer recording medium |
US4756950A (en) * | 1985-03-23 | 1988-07-12 | Mitsubishi Paper Mills, Ltd. | Gradation recording heat-transfer sheet |
US4783360A (en) * | 1985-07-22 | 1988-11-08 | Canon Kabushiki Kaisha | Thermal transfer material |
GB2178553B (en) * | 1985-07-29 | 1990-01-04 | Canon Kk | Thermal transfer material |
JPH07421B1 (en) * | 1985-12-17 | 1995-01-11 | ||
JPH0767831B2 (en) * | 1986-04-18 | 1995-07-26 | 株式会社リコー | Thermal transfer recording medium |
US4818605A (en) * | 1986-04-18 | 1989-04-04 | Ricoh Company, Ltd. | Thermosensitive image transfer recording medium |
DE3635141C1 (en) * | 1986-10-15 | 1988-03-03 | Pelikan Ag | Thermocarbon tape with a plastic-bound melting ink and a process for producing this tape |
DE3728075A1 (en) * | 1987-08-22 | 1989-03-02 | Pelikan Ag | THERMOFIBB BAND FOR THERMAL TRANSFER PRESSURE AND ITS MANUFACTURE |
US4894283A (en) * | 1988-05-10 | 1990-01-16 | Ncr Corporation | Reuseable thermal transfer ribbon |
JP3242340B2 (en) * | 1996-02-09 | 2001-12-25 | 東芝テック株式会社 | Transfer type thermal printer |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58183297A (en) * | 1982-04-22 | 1983-10-26 | Mitsubishi Electric Corp | Multiple heat transfer sheet for gradation recording and preparation thereof |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3119014A (en) * | 1960-12-09 | 1964-01-21 | Columbia Ribbon & Carbon | Novel duplicating system |
DE3007330A1 (en) * | 1980-02-27 | 1981-09-03 | Ibm Deutschland Gmbh, 7000 Stuttgart | METHOD FOR PRODUCING A RECORD CARRIER COATED WITH A CONTRASTANT-CONTAINING VARNISH LAYER AND ALUMINUM-CONTAINING LAYER, AND RECORD CARTRIDGE PRODUCED BY THIS |
DE3017449A1 (en) * | 1980-05-07 | 1981-11-12 | Robert Bosch Gmbh, 7000 Stuttgart | REGISTRATION METAL PAPER |
JPS57160691A (en) * | 1981-03-31 | 1982-10-04 | Fujitsu Ltd | Ink composition for heat transfer recording and heat transfer recording ink sheet employing said composition |
-
1984
- 1984-06-26 JP JP59131455A patent/JPS6110490A/en active Granted
-
1985
- 1985-06-19 US US06/746,352 patent/US4612243A/en not_active Expired - Fee Related
- 1985-06-20 CA CA000484631A patent/CA1237280A/en not_active Expired
- 1985-06-21 DE DE19853522316 patent/DE3522316A1/en not_active Ceased
- 1985-06-21 DK DK280785A patent/DK280785A/en not_active Application Discontinuation
- 1985-06-24 GB GB8515963A patent/GB2161950B/en not_active Expired
- 1985-06-24 SE SE8503124A patent/SE467818B/en not_active IP Right Cessation
- 1985-06-24 AU AU43996/85A patent/AU585868B2/en not_active Ceased
- 1985-06-25 CH CH2697/85A patent/CH670422A5/de not_active IP Right Cessation
- 1985-06-25 IT IT2127585A patent/IT1200648B/en active
- 1985-06-26 KR KR8504559A patent/KR900005831B1/en not_active IP Right Cessation
- 1985-06-26 FR FR8509729A patent/FR2566328B1/en not_active Expired
- 1985-06-26 NL NL8501842A patent/NL8501842A/en not_active Application Discontinuation
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58183297A (en) * | 1982-04-22 | 1983-10-26 | Mitsubishi Electric Corp | Multiple heat transfer sheet for gradation recording and preparation thereof |
Also Published As
Publication number | Publication date |
---|---|
FR2566328B1 (en) | 1989-11-17 |
CH670422A5 (en) | 1989-06-15 |
DK280785D0 (en) | 1985-06-21 |
IT8521275A0 (en) | 1985-06-25 |
JPS6110490A (en) | 1986-01-17 |
AU4399685A (en) | 1986-01-02 |
AU585868B2 (en) | 1989-06-29 |
SE467818B (en) | 1992-09-21 |
SE8503124L (en) | 1985-12-27 |
KR860000156A (en) | 1986-01-25 |
DK280785A (en) | 1985-12-27 |
IT1200648B (en) | 1989-01-27 |
FR2566328A1 (en) | 1985-12-27 |
NL8501842A (en) | 1986-01-16 |
GB2161950B (en) | 1987-10-28 |
GB8515963D0 (en) | 1985-07-24 |
KR900005831B1 (en) | 1990-08-13 |
GB2161950A (en) | 1986-01-22 |
DE3522316A1 (en) | 1986-01-02 |
SE8503124D0 (en) | 1985-06-24 |
US4612243A (en) | 1986-09-16 |
CA1237280A (en) | 1988-05-31 |
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